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新生儿戒断综合征中舌下含服丁丙诺啡的群体药代动力学模型

Population Pharmacokinetic Model of Sublingual Buprenorphine in Neonatal Abstinence Syndrome.

作者信息

Ng Chee M, Dombrowsky Erin, Lin Hopi, Erlich Michelle E, Moody David E, Barrett Jeffrey S, Kraft Walter K

机构信息

Clinical Pharmacology and Therapeutics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Department of Pediatrics, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Pharmacotherapy. 2015 Jul;35(7):670-80. doi: 10.1002/phar.1610. Epub 2015 Jul 14.

Abstract

OBJECTIVE

Neonatal abstinence syndrome (NAS)--a clinical entity of infants from in utero exposure to psychoactive xenobiotic and buprenorphine--has been successfully used to treat NAS. However, nothing is known about the pharmacokinetics (PK) of buprenorphine in neonates with NAS. To our knowledge, this is the first study to investigate the population pharmacokinetic of sublingual buprenorphine in neonates with NAS.

DESIGN

A retrospective population PK analysis of: (1) neonates with NAS treated with sublingual buprenorphine in randomized, double blinded clinical study and (2) data from healthy adults from a previously published pharmacokinetic study.

SETTING

Neonatal intensive care unit and general clinical research unit.

PATIENTS

Twenty-four neonates with NAS and five healthy adults.

INTERVENTIONS

All participants received sublingual buprenorphine per study protocol.

MEASUREMENTS AND MAIN RESULTS

A total of 303 PK data from 29 neonates and adults were used for model development. A population pharmacokinetic analysis was conducted using a first order conditional estimation with interaction in the NONMEM software program. A two-compartment linear PK model with first-order absorption process best described the pharmacokinetics of sublingual buprenorphine in neonates. The apparent clearance (CL) of buprenorphine was linearly related to body weight and matured with increasing age via two distinct saturated pathways. A typical neonate with NAS (body weight, 2.9 kg; postnatal age; 5.4 days) had a CL of 3.5 L/kg/hour and elimination half-life of 11 hours. Phenobarbital did not affect the clearance of buprenorphine compared to neonates of similar age and weight.

CONCLUSIONS

This is the first study to investigate the population PK of sublingual buprenorphine in neonatal NAS. To our knowledge, this is also the first report to describe the age-dependent changes of buprenorphine PK in this patient population. No buprenorphine dose adjustment is needed for neonates with NAS treated with buprenorphine and concurrent phenobarbital.

摘要

目的

新生儿戒断综合征(NAS)——一种因胎儿在子宫内接触精神活性外源性物质和丁丙诺啡而导致的临床病症——已成功用于治疗NAS。然而,关于丁丙诺啡在患有NAS的新生儿中的药代动力学(PK)情况却一无所知。据我们所知,这是第一项研究丁丙诺啡舌下含服在患有NAS的新生儿中的群体药代动力学的研究。

设计

一项回顾性群体PK分析,包括:(1)在随机、双盲临床研究中接受丁丙诺啡舌下含服治疗的患有NAS的新生儿,以及(2)来自先前发表的药代动力学研究中的健康成年人的数据。

地点

新生儿重症监护病房和普通临床研究单位。

患者

24名患有NAS的新生儿和5名健康成年人。

干预措施

所有参与者均按照研究方案接受丁丙诺啡舌下含服。

测量和主要结果

来自29名新生儿和成年人的总共303个PK数据用于模型开发。使用NONMEM软件程序中的带交互作用的一阶条件估计进行群体药代动力学分析。具有一级吸收过程的二室线性PK模型最能描述丁丙诺啡舌下含服在新生儿中的药代动力学。丁丙诺啡的表观清除率(CL)与体重呈线性相关,并通过两条不同的饱和途径随年龄增长而成熟。一名典型的患有NAS的新生儿(体重2.9千克;出生后年龄5.4天)的CL为3.5升/千克/小时,消除半衰期为11小时。与年龄和体重相似的新生儿相比,苯巴比妥不影响丁丙诺啡的清除率。

结论

这是第一项研究丁丙诺啡舌下含服在新生儿NAS中的群体PK的研究。据我们所知,这也是第一份描述该患者群体中丁丙诺啡PK的年龄依赖性变化的报告。对于接受丁丙诺啡和同时使用苯巴比妥治疗的患有NAS的新生儿,无需调整丁丙诺啡剂量。

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